Canonical Allele Identifier: CA2617597696

Gene: CLEC12B

Linked Data

• gnomAD v4: 12-10017772-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.10017773del , CM000674.2:g.10017773del	GRCh38
NC_000012.11:g.10170372del , CM000674.1:g.10170372del	GRCh37
NC_000012.10:g.10061639del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338896.11:c.681-558del MANE Select	ENSP00000344563.5:n.681-558del
ENST00000338896.10:c.681-558del	ENSP00000344563.5:n.681-558del
ENST00000338896.9:c.681-558del	ENSP00000344563.5:n.681-558del
ENST00000396502.5:c.*2027del	ENSP00000379759.1:n.*2027del
ENST00000539155.1:c.*2520del	ENSP00000444909.1:n.*2520del
ENST00000544853.5:c.*129-558del	ENSP00000439561.1:n.*129-558del
NM_001129998.1:c.681-558del	NP_001123470.1:n.681-558del
NM_205852.2:c.*2027del	NP_995324.2:n.*2027del
NR_120484.1:n.249-2000del
XM_006719070.2:c.681-645del	XP_006719133.1:n.681-645del
XM_006719071.2:c.*3-558del	XP_006719134.1:n.*3-558del
XM_006719072.1:c.*800del	XP_006719135.1:n.*800del
XM_011520658.1:c.654-558del	XP_011518960.1:n.654-558del
XM_011520659.1:c.*776del	XP_011518961.1:n.*776del
XM_011520660.1:c.*771del	XP_011518962.1:n.*771del
XM_011520661.1:c.*10-558del	XP_011518963.1:n.*10-558del
XM_011520662.1:c.*807del	XP_011518964.1:n.*807del
XM_011520663.1:c.526-558del	XP_011518965.1:n.526-558del
XM_011520664.1:c.526-645del	XP_011518966.1:n.526-645del
XR_242889.3:n.956-558del
XR_931290.1:n.1753del
NM_001129998.2:c.681-558del	NP_001123470.1:n.681-558del
NM_001319241.1:c.372-558del	NP_001306170.1:n.372-558del
NM_001319242.1:c.*2027del	NP_001306171.1:n.*2027del
NM_205852.3:c.*2027del	NP_995324.2:n.*2027del
NR_135049.1:n.961-558del
XM_011520658.2:c.654-558del	XP_011518960.1:n.654-558del
XM_011520663.2:c.526-558del	XP_011518965.1:n.526-558del
XM_017019295.1:c.372-558del	XP_016874784.1:n.372-558del
XM_024448976.1:c.681-645del	XP_024304744.1:n.681-645del
XM_024448977.1:c.*2034del	XP_024304745.1:n.*2034del
XR_002957401.1:n.106-1625del
NM_001129998.3:c.681-558del MANE Select	NP_001123470.1:n.681-558del
NM_001387138.1:c.681-645del	NP_001374067.1:n.681-645del
NR_169587.1:n.258-1625del